Terbium doped phosphate-based green luminescent material and preparation method thereof

ABSTRACT

Terbium doped phosphate-based green luminescent material and preparation method thereof are provided. The chemical formula of the material is M 3 RE 1-x Tb x (PO 4 ) 3 , wherein, M is alkaline-earth metals, RE is rare-earth elements, x is in a range of 0.001 to 1. The preparation method of the material includes the following steps; providing the compound used as the source of alkaline earth metal, the compound used as the source of phosphate, the compound used as the source of rare-earth, and the compound used as the source of Tb 3+  according to the molar ratio of the elements in M 3 RE 1-x Tb x (PO 4 ) 3 , wherein, the compound used as the source of phosphate is added at excess molar ratio in a range of 10% to 30%; mixing and grinding the compound to get mixture; sintering the mixture as pre-treatment, and then cooling the mixture to get a sintered matter; grinding; calcining in reducing atmosphere, and then cooling them.

FIELD OF THE INVENTION

The present disclosure relates to luminescent materials, especially to a terbium doped phosphate-based green luminescent material which can be excited by vacuum ultraviolet light and a preparation method thereof.

BACKGROUND OF THE INVENTION

Recently, With increasing emphasis on environmental protection, mercury-free light source has become one of important direction of the study. Xenon (Xe) discharging is now the main excited light. Xe radiation may produce a light having a wavelength of 147 nm or 172 nm which can excite luminescent material. To improve energy utilization of the Xe radiation, a suitable luminescent material is necessary to be developed. The suitable luminescent material can effectively absorb the 172 nm light and convert the 172 nm light to a visible light. Now the main commercial luminescent materials are Y₂O₃:Eu³⁺, (Y, Gd)BO₃:Eu³⁺ (both of them are red luminescent materials), Zn₂SiO₄:Mn²⁺, BaAl₁₂O₁₉:Mn²⁺ (both of them are green luminescent materials), and BaMgAl₁₀O₁₇:Eu²⁺ (blue luminescent materials). However, the green luminescent materials, the Zn₂SiO₄:Mn²⁺ and the BaAl₁₂O₁₉:Mn²⁺ both have long afterglow time, which negatively affect the display of dynamic images.

Basically in luminescence mechanism, the luminescent materials emits visible light by absorbing vacuum ultraviolet light (VUV) and then transiting the energy to luminescent ions of the luminescent material which emits light. Accordingly, the luminescent material may have a more effective emitting by improving the absorption of VUV and the energy transition of the material. That is, the sensitized groups contained in the material, such as negative ion groups, can be utilized to sensitize luminescent ions to improve the emitting property. In the negative ion groups, an isolated PO₄ ³⁻ group, has a space P—O tetrahedral structure and a strong absorption to the 150 nm-175 nm light. The phosphates, such as Sr₃Y(PO₄)₃, Ca₃Y(PO₄)₃, Ba₃La(PO₄)₃, Ca₃La(PO₄)₃, Sr₃La(PO₄)₃, and Ca₃Gd(PO₄)₃, all contain isolated space P—O tetrahedral structures. These phosphates have excellent stabilities and vacuum ultraviolet radiation resistance. The green luminescent materials having luminescence centers of terbium ions (Tb³⁺) have been widely used. These Tb³⁺ contained green luminescent materials, such as Ca₅(PO₄)₃F:Tb³⁺, Na₂GdPO₄F₂:Tb³⁺, NaGd(PO₃)₄:Tb³⁺, and La(PO₃)₃:Tb³⁺, have high luminescence intensity and short fluorescence life time.

However, there are none of disclosure of the luminescent materials, such as, Sr₃Y(PO)₃, Ca₃Y(PO₄)₃, Ba₃La(PO₄)₃, Ca₃La(PO₄)₃, Sr₃La(PO₄)₃, and Ca₃Gd(PO₄)₃:Tb³⁺, all of which can be excited by VUV.

SUMMARY OF THE INVENTION

The technical problem of the present invention to be solved is to provide terbium doped phosphate-based green luminescent material which has high luminescence intensity, and preparation method for the material. The method is simple, environmental friendly, easy to be controlled, and can be effectively implemented in industry.

The technical solution to solve the technical problem in the present invention is: providing terbium doped phosphate-based green luminescent material, the said terbium doped phosphate-based green luminescent material has chemical formula of M₃RE_(1-x)Tb_(x)(PO₄)₃, wherein, M is alkaline-earth metal, RE is rare-earth element, and x is in a range of 0.001 to 1.

And, preparation method of terbium doped phosphate-based green luminescent material, comprises:

Step one, providing the compound used as the source of alkaline earth metal, the compound used as the source of phosphate, the compound used as the source of rare-earth, and the compound used as the source of Tb³⁺ according to the molar ration of the elements in M₃RE_(1-x)Tb_(x)(PO₄)₃, wherein the compound used as the source of phosphate is added at excess molar ratio in a range of 10% to 30%, M is alkaline earth metal, RE is rare-earth element, and x is in a range of 0.001 to 1;

Step two, mixing and grinding the compounds to get a mixture;

Step three, sintering the mixture as pre-treatment, and then cooling the mixture to get a sintered matter;

Step four, grinding the sintered matter, calcining the grinded matter in reducing atmosphere and then cooling them to get the terbium doped phosphate-based green luminescent material.

In the exemplary embodiment, the terbium doped phosphate-based green luminescent material formed by the sintering process and the calcining process has a strong absorption of the 172 nm light. The exemplary material can be used as a green luminescent material in PDP or mercury-free fluorescent lamps.

Compared to the present technology, the invention has the advantages of: 1. the terbium doped phosphate-based green luminescent material not only has a strong absorption of the 172 nm light, the terbium doped phosphate-based green luminescent material of the exemplary embodiment further has a short fluorescence life time. When the terbium doped phosphate-based green luminescent material is Ca₃La_(0.95)Tb_(0.05)(PO₄)₃ the fluorescence life time is about 2.46 ms, which is lower than the commercial BaAl₁₂O₁₉:Mn. 2. The terbium doped phosphate-based green luminescent material of the exemplary embodiment has a higher luminescence intensity than that of the commercial BaAl₁₂O₁₉:Mn. 3. The preparation method of terbium doped phosphate-based green luminescent material is simply, environmental friendly, easy controlled, and can be commercially processed.

BRIEF DESCRIPTION OF THE DRAWINGS

Further description of the present invention will be illustrated, which combined with drawings and embodiments in the drawings.

FIG.1 shows an excitation spectrum of the Ca₃La_(0.95)Tb_(0.05)(PO₄)₃ of example 1, the excitation spectrum is tested with a monitoring wavelength of about 543 nm;

FIG. 2 shows emission spectrums of the Ca₃La_(0.95)Tb_(0.05)(PO₄)₃ of example 1 and a commercial BaAl₁₂O₁₉:Mn, the emission spectrums are tested with an excitation wavelength of about 172 nm;

FIG. 3 shows a fluorescence life time test of the Ca₃La_(0.95)Tb_(0.05)(PO₄)₃ of example 1, the fluorescence life time is tested with an excitation wavelength of about 378 nm and a monitoring wavelength of about 543 nm;

FIG. 4 shows a flow chat of preparation method of the terbium doped phosphate-based green luminescent material.

DETAILED DESCRIPTION OF ILLUSTRATED EMBODIMENTS

The examples hereinafter described merely being preferred or exemplary embodiment of the disclosure. It will be apparent that various changes may be made thereto without departing from the spirit and scope of the disclosure.

According to an embodiment, a terbium doped phosphate-based green luminescent material has chemical formula of M₃RE_(1-x)Tb_(x)(PO₄)₃, wherein, M is alkaline earth metal, RE is rare-earth element, and x is in a range of 0.001 to 1. The rare-earth element RE is at least one of the gadolinium (Gd), yttrium (Y), and lanthanum (La). The alkaline earth metal M is at least one of the calcium (Ca), strontium (Sr), and barium (Ba).

In the terbium doped phosphate-based green luminescent material, M₃RE(PO₄)₃ is the matrix of the terbium doped phosphate-based green luminescent material, as a metaphosphate, the M₃RE(PO₄)₃ has a strong vacuum ultraviolet radiation resistance. When Tb³⁺ is doped to the M₃RE(PO₄)₃, the luminescence mechanism of the M₃RE(PO₄)₃ is: one aspect, the Tb³⁺ in the material has a f-d transition at a wavelength in a range of 170 nm to 220 nm, between which the material absorbs the 172 nm light, on the other hand, the matrix of the material has a strong absorption of the 150 nm-175 nm vacuum ultraviolet light (VUV), for the f-d transition of the Tb³⁺ is just posited between the 150 nm-175 nm wavelengths, thus the energy absorbed by the matrix can be effectively transited to the Tb³⁺ to emit green light. As such, the utilization of the VUV of the material is improved and the luminescence intensity of the Tb³⁺ is enhanced.

Referring to FIG. 4, a preparation method of the terbium doped phosphate-based green luminescent material includes the following steps;

S01, the compound used as the source of alkaline earth metal, the compound used as the source of phosphate, the compound used as the source of rare-earth, and the compound used as the source of Tb³⁺ according to the molar ratio of the elements in M₃RE_(1-x)Tb_(x)(PO₄)₃ are provided. The compound used as the source of phosphate is added at excess molar ratio in a range of 10%-30%. M is alkaline earth metal, RE is rare-earth element, and x is in a range of 0.001 to 1;

S02, the compounds are mixed and grinded in an agate mortar to get a mixture;

S03, the mixture is sintered as pre-treatment, and then cooled to get a sintered matter;

S04, the sintered matter is removed out and grinded. The grinded matter is then calcined in reducing atmosphere and then cooled to get the terbium doped phosphate-based green luminescent material.

In step S01, the compound used as the source of alkaline earth metal is at least one of alkaline earth oxide, alkaline earth hydroxide, alkaline earth carbonate, and alkaline earth oxalate. The compound used as the source of phosphate is at least one of diammonium phosphate and ammonium dihydrogen phosphate. The compound used as the source of RE³⁺ is rare-earth oxide, rare-earth nitrate, or rare-earth oxalate. All of the compounds are provided according to the molar ratio of the elements in the M₃RE_(1-x)Tb_(x)(PO₄)₃. The compound used as the source of phosphate is added at excess molar ratio in a range of 10% to 30%, optimal selection of 20% in the embodiment.

In step S03, the mixture is sintered in a corundum crucible (not shown) at the temperature in a range of 300° C. to 700° C. for 1 hour to 6 hours. The sintered matter is then cooled to room temperature.

In step S04, the sintered matter is grinded and then calcined in a reducing atmosphere to get the terbium doped phosphate-based green luminescent material. Specially, the calcining process includes a first calcining process and a second calcining process. The first calcining process is carried out in an oven (not shown) at the temperature in a range of 800° C. to 1500° C. for 4 hours to 24 hours. The first calcining process is followed by a cooling process and a grinding process. The second calcining process is carried out in the oven at the temperature in a range of 700° C. to 950° C. for 5 hours to 10 hours. At least one of the first and the second calcining processes is carried out in a reducing atmosphere. The reducing atmosphere is the mixing gases of the nitrogen and the hydrogen, the hydrogen, or the carbon monoxide.

Special examples are disclosed as follows to demonstrate the terbium doped phosphate-base green luminescent material and preparation method for making the same. In the examples, the rare-earth oxide, the rare-earth nitrate, and the rare-earth oxalate all have a purity of more than 4N. The diammonium phosphate and the ammonium dihydrogen phosphate are both chemically pure. The reducing atmosphere is the mixing gases of the nitrogen and the hydrogen having a volume ratio of 95:5 or 90:10, the hydrogen, or the carbon monoxide.

EXAMPLE 1

0.9008 g calcium carbonate (CaCO₃), 1.2422 g ammonium dihydrogen phosphate (NH₄H₂PO₄) (at excess molar ratio of 20%), 0.0279 g terbium oxide (Tb₄O₇), and 0.4645 g lanthanum oxide (La₂O₃) are provided and positioned in an agate mortar to be grinded. The grinded matter is sintered in a corundum crucible at 500° C. for 3 hours and then naturally cooled to room temperature. The cooled sintered matter is grinded completely. After that, the sintered matter is firstly calcined at 1300° C. for 10 hours in a reducing atmosphere and then cooled to room temperature. The reducing atmosphere is a mixing gas of N₂ and H₂ having a volume ratio of 95:5. The first calcined matter is grinded once more and secondly calcined at 900° C. for 5 hours, followed by a cooling process and a grinding process. As such, white powders of terbium doped phosphate-based green luminescent material of Ca₃La_(0.95)Tb_(0.05)(PO₄)₃ are obtained.

EXAMPLE 2

1.3287 g strontium carbonate (SrCO₃), 1.2423 g ammonium dihydrogen phosphate (NH₄H₂PO₄) (at excess molar ratio of 20%), 0.0281 g terbium oxide (Tb₄O₇), and 0.4643 g lanthanum oxide (La₂O₃) are provided and positioned in an agate mortar to be grinded. The grinded matter is sintered in a corundum crucible at 300° C. for 6 hours and then naturally cooled to room temperature. The cooled sintered matter is grinded completely. After that, the sintered matter is firstly calcined at 1250° C. for 8 hours in a reducing atmosphere and then cooled to room temperature. The reducing atmosphere is a mixing gas of N₂ and H₂ having a volume ratio of 95:5. The first calcined matter is grinded once more and then secondly calcined at 900° C. for 7 hours, followed by a cooling process and a grinding process. As such, white powders of terbium doped phosphate-based green luminescent material of Sr₃La_(0.95)Tb_(0.05)(PO₄)₃ are obtained.

EXAMPLE 3

1.7786 g barium carbonate (BaCO₃), 1.2422 g ammonium dihydrogen phosphate (NH₄H₂PO₄) (at excess molar ratio of 20%), 0.0280 g terbium oxide (Tb₄O₇), and 0.4645 g lanthanum oxide (La₂O₃) are provided and positioned in an agate mortar to be grinded. The grinded matter is sintered in a corundum crucible at 700° C. for 1 hour and then naturally cooled to room temperature. The cooled sintered matter is grinded completely. After that, the sintered matter is firstly calcined at 950° C. for 8 hours in a reducing atmosphere and then cooled to room temperature. The reducing atmosphere is a mixing gas of N₂ and H₂ having a volume ratio of 95:5. The first calcined matter is grinded once more and then secondly calcined at 900° C. for 6 hours, followed by a cooling process and a grinding process. As such, white powders of terbium doped phosphate-based green luminescent material of Ba₃La_(0.95)Tb_(0.05)(PO₄)₃ are obtained.

EXAMPLE 4

1.3287 g strontium carbonate (SrCO₃), 1.2423 g ammonium dihydrogen phosphate (NH₄H₂PO₄) (at excess molar ratio of 20%), 0.0561 g terbium oxide (Tb₄O₇), and 0.4398 g lanthanum oxide (La₂O₃) are provided and positioned in an agate mortar to be grinded. The grinded matter is sintered in a corundum crucible at 300° C. for 4 hours and then naturally cooled to room temperature. The cooled sintered matter is grinded completely. After that, the sintered matter is firstly calcined at 800° C. for 12 hours in a reducing atmosphere and then cooled to room temperature. The reducing atmosphere is a mixing gas of N₂ and H₂ having a volume ratio of 95:5. The first calcined matter is grinded once more and secondly calcined at 800° C. for 7 hours at a reducing atmosphere of H₂, followed by a cooling process and a grinding process. As such, white powders of terbium doped phosphate-based green luminescent material of Sr₃La_(0.09)Tb_(0.10)(PO₄)₃ are obtained.

EXAMPLE 5

1.7786 g barium carbonate (BaCO₃), 1.2423 g ammonium dihydrogen phosphate (NH₄H₂PO₄) (at excess molar ratio of 20%), and 0.5606 g terbium oxide (Tb₄O₇) are provided and positioned in an agate mortar to be grinded. The grinded matter is sintered in a corundum crucible at 600° C. for 4 hours and then naturally cooled to room temperature. The cooled sintered matter is grinded completely. After that, the sintered matter is firstly calcined at 950° C. for 8 hours and then cooled to room temperature. The first calcined matter is grinded once more and secondly calcined at 900° C. for 6 hours in a reducing atmosphere of H₂, followed by a cooling process and a grinding process. As such, white powders of terbium doped phosphate-based green luminescent material of Ba₃Tb(PO₄)₃ are obtained.

EXAMPLE 6

0.5046 g calcium oxide (CaO), 1.2423 g ammonium dihydrogen phosphate (NH₄H₂PO₄) (at excess molar ratio of 20%), and 0.5606 g terbium oxide (Tb₄O₇) are provided and positioned in an agate mortar to be grinded. The grinded matter is sintered in a corundum crucible at 500° C. for 3 hours and then naturally cooled to room temperature. The cooled sintered matter is grinded completely. After that, the sintered matter is firstly calcined at 1200° C. for 10 hours in a reducing atmosphere of CO and then cooled to room temperature. The first calcined matter is grinded once more and secondly calcined at 900° C. for 5 hours, followed by a cooling process and a grinding process. As such, white powders of terbium doped phosphate-based green luminescent material of Ca₃Tb(PO₄)₃ are obtained.

EXAMPLE 7

1.3287 g strontium carbonate (SrCO₃), 1.2423 g ammonium dihydrogen phosphate (NH₄H₂PO₄) (at excess molar ratio of 20%), 0.0841 g terbium oxide (Tb₄O₇), and 0.4155 g lanthanum oxide (La₂O₃) are provided and positioned in an agate mortar to be grinded. The grinded matter is sintered in a corundum crucible at 500° C. for 4 hours and then naturally cooled to room temperature. The cooled sintered matter is grinded completely. After that, the sintered matter is firstly calcined at 1200° C. for 8 hours in a reducing atmosphere of H₂ and then cooled to room temperature. The first calcined matter is grinded once more and secondly calcined at 900° C. for 7 hours, followed by a cooling process and a grinding process. As such, white powders of terbium doped phosphate-based green luminescent material of Sr₃La_(0.85)Tb_(0.15)(PO₄)₃ are obtained.

EXAMPLE 8

1.3287 g strontium carbonate (SrCO₃), 1.2423 g ammonium dihydrogen phosphate (NH₄H₂PO₄) (at excess molar ratio of 20%), 0.0841 g terbium oxide (Tb₄O₇), and 0.2880 g yttrium oxide (Y₂O₃) are provided and positioned in an agate mortar to be grinded. The grinded matter is sintered in a corundum crucible at 500° C. for 4 hours and then naturally cooled to room temperature. The cooled sintered matter is grinded completely. After that, the sintered matter is firstly calcined at 110° C. for 8 hours in a reducing atmosphere of CO and then cooled to room temperature. The first calcined matter is grinded once more and secondly calcined at 900° C. for 7 hours, followed by a cooling process and a grinding process. As such, white powders of terbium doped phosphate-based green luminescent material of Sr₃Y_(0.85)Tb_(0.15)(PO₄)₃ are obtained.

EXAMPLE 9

0.9008 g calcium carbonate (CaCO₃), 1.2423 g ammonium dihydrogen phosphate (NH₄H₂PO₄) (at excess molar ratio of 20%), 0.0841 g terbium oxide (Tb₄O₇), and 1.1507 g six gadolinium nitrate hydrate (Gd(NO₃)₃.6H₂O) are provided and positioned in an agate mortar to be grinded. The grinded matter is sintered in a corundum crucible at 500° C. for 4 hours and then naturally cooled to room temperature. The cooled sintered matter is grinded completely. After that, the sintered matter is firstly calcined at 1000° C. for 8 hours in a reducing atmosphere of CO and then cooled to room temperature. The first calcined matter is grinded once more and secondly calcined at 900° C. for 7 hours in a reducing atmosphere of N₂ and H₂, followed by a cooling process and a grinding process. The volume ratio of the N₂ and the H₂ is 90:10. As such, white powders of terbium doped phosphate-based green luminescent material of Ca₃Gd_(0.85)Tb_(0.15)(PO₄)₃ are obtained.

EXAMPLE 10

0.6668 g calcium hydroxide (Ca(OH)₂), 1.3458 g ammonium dihydrogen phosphate (NH₄H₂PO₄) (at excess molar ratio of 30%), 0.0841 g terbium oxide (Tb₄O₇), and 0.2880 g yttrium (Y₂O₃) are provided and positioned in an agate mortar to be grinded. The grinded matter is sintered in a corundum crucible at 500° C. for 4 hours and then naturally cooled to room temperature. The cooled sintered matter is grinded completely. After that, the sintered matter is firstly calcined at 1000° C. for 8 hours in a reducing atmosphere of H₂ and then cooled to room temperature. The first calcined matter is grinded once more and secondly calcined at 900° C. for 7 hours, followed by a cooling process and a grinding process. As such, white powders of terbium doped phosphate-based green luminescent material of Ca₃Y_(0.85)Tb_(0.15)(PO₄)₃ are obtained.

EXAMPLE 11

1.1529 g calcium oxalate (CaC₂O₄), 1.3074 g diammonium phosphate (NH₄)₂HPO₄) (at excess molar ratio of 10%), 0.0436 g terbium oxalate (Tb₂(C₂O₄)₃), and 0.4643 g lanthanum oxide (La₂O₃) are provided and positioned in an agate mortar to be grinded. The grinded matter is sintered in a corundum crucible at 500° C. for 3 hours and then naturally cooled to room temperature. The cooled sintered matter is grinded completely. After that, the sintered matter is firstly calcined at 1300° C. for 10 hours in a reducing atmosphere of N₂ and H₂ and then cooled to room temperature. The volume ratio of the N₂ and H₂ is 95:5. The first calcined matter is grinded once more and secondly calcined at 700° C. for 10 hours, followed by a cooling process and a grinding process. As such, white powders of terbium doped phosphate-based green luminescent material of Ca₃La_(0.95)Tb_(0.05)(PO₄)₃ are obtained.

EXAMPLE 12

1.7428 g strontium oxalate monohydrate (SrC₂O₄.H₂O), 1.2423 g diammonium phosphate (NH₄)₂HPO₄) (at excess molar ratio of 20%), 0.0841 g terbium oxide (Tb₄O₇), and 0.9672 g ten gadolinium oxalate hydrate (Gd₂(C₂O₄)₃.10H₂O) are provided and positioned in an agate mortar to be grinded. The grinded matter is sintered in a corundum crucible at 500° C. for 4 hours and then naturally cooled to room temperature. The cooled sintered matter is grinded completely. After that, the sintered matter is firstly calcined at 800° C. for 24 hours in a reducing atmosphere of CO and then cooled to room temperature. The first calcined matter is grinded once more and secondly calcined at 900° C. for 7 hours in a reducing atmosphere of N₂ and H₂, followed by a cooling process and a grinding process. The volume ratio of the N₂ and H₂ is 90:10. As such, white powders of terbium doped phosphate-based green luminescent material of Sr₃Gd_(0.85)Tb_(0.15)(PO₄)₃ are obtained.

EXAMPLE 13

1.3287 g strontium carbonate (SrCO₃), 1.4262 g diammonium phosphate (NH₄)₂HPO₄) (at excess molar ratio of 20%), 0.0014 g six terbium nitrate hydrate (Tb(NO₃)₃).6H₂O, and 0.4882 g lanthanum oxide (La₂O₃) are provided and positioned in an agate mortar to be grinded. The grinded matter is sintered in a corundum crucible at 500° C. for 4 hours and then naturally cooled to room temperature. The cooled sintered matter is grinded completely. After that, the sintered matter is firstly calcined at 1500° C. for 4 hours in a reducing atmosphere of N₂ and H₂ and then cooled to room temperature. The volume ratio of the N₂ and H₂ is 95:5. The first calcined matter is grinded once more and secondly calcined at 950° C. for 5 hours, followed by a cooling process and a grinding process. As such, white powders of terbium doped phosphate-based green luminescent material of Sr₃La_(0.999)Tb_(0.001)(PO₄)₃ are obtained.

EXAMPLE 14

0.4504 g calcium carbonate (CaCO₃), 0.3321 g strontium carbonate (SrCO₃), 0.4440 g barium carbonate (BaCO₃), 1.2422 g ammonium dihydrogen phosphate NH₄H ₂PO₄ (at excess molar ratio of 20%), 0.0279 g terbium oxide (Tb₄O₇), 0.0517 g gadolinium oxide (Gd₂O₃), and 0.4179 g lanthanum oxide (La₂O₃) are provided and positioned in an agate mortar to be grinded. The grinded matter is sintered in a corundum crucible at 500° C. for 3 hours and then naturally cooled to room temperature. The cooled sintered matter is grinded completely. After that, the sintered matter is firstly calcined at 1300° C. for 10 hours in a reducing atmosphere of N₂ and H₂ and then cooled to room temperature. The volume ratio of the N₂ and H₂ is 90:10. The first calcined matter is grinded once more and secondly calcined at 900° C. for 5 hours, followed by a cooling process and a grinding process. As such, whithe powders of terbium doped phosphate-based green luminescent material of (Ca_(0.50)Sr_(0.25)Ba_(0.25))₃(La_(0.90)Gd_(0.10))_(0.95)Tb_(0.05(PO) ₄)₃ are obtained.

EXAMPLE 15

0.8558 g calcium carbonate (CaCO₃), 0.0888 g barium carbonate (BaCO₃), 1.2422 g ammonium dihydrogen phosphate NH₄H₂PO₄ (at excess molar ratio of 20%), 0.0279 g terbium oxide (Tb₄O₇), 0.1609 g yttrium oxide (Y2O3), 0.0517 g gadolinium oxide (Gd₂O₃), and 0.1857 g lanthanum oxide (La₂O₃) are provided and positioned in an agate mortar to be grinded. The grinded matter is sintered in a corundum crucible at 500° C. for 3 hours and then naturally cooled to room temperature. The cooled sintered matter is grinded completely. After that, the sintered matter is firstly calcined at 1200 ° C. for 10 hours in a reducing atmosphere of N₂ and H₂ and then cooled to room temperature. The volume ratio of the N₂ and H₂ is 90:10. The first calcined matter is grinded once more and secondly calcined at 900° C. for 5 hours, followed by a cooling process and a grinding process. As such, white powders of terbium doped phosphate-based green luminescent material of (Ca_(0.95)Ba_(0.05))₃(Y_(0.5)La_(0.40)Gd_(0.10))_(0.95)Tb_(0.05)(PO₄)₃ are obtained.

FIG.1 shows an excitation spectrum of the Ca₃La_(0.95)Tb_(0.05)(PO₄)₃ of example 1. The excitation spectrum is test with a monitoring wavelength of 543 nm. There are two wave crests in the excitation spectrum of the Ca₃La_(0.95)Tb_(0.05)(PO₄)₃. The two wave crests locate at a wave length between about 150 nm to about 250 nm, indicating that the Ca₃La_(0.95)Tb_(0.05)(PO₄)₃ has a strong absorption of the vacuum ultraviolet light which has a wave length from about 150 nm to about 250 nm. The Ca₃La_(0.95)Tb_(0.05)(PO₄)₃ can be excited by the 172 nm light produced by Xe, and can be used in PDP or mercury-free fluorescent lamps.

FIG. 2 shows an emission spectrum (referring to the solid line) of the Ca₃La_(0.95)Tb_(0.05)(PO₄)₃ of example 1 excited by the 172 nm light, and an emission spectrum (referring to the broken line) of a commercial BaAl₁₂O₁₉:Mn excited by the 172 nm light. The two emission spectrums indicate that the Ca₃La_(0.95)Tb_(0.05)(PO₄)₃ has a luminescence intensity much greater than that of the commercial BaAl₁₂O₁₉:Mn.

FIG. 3 shows a fluorescence life time test of the Ca₃La_(0.95)Tb_(0.05)(PO₄)₃ of example 1. The fluorescence life time is tested with an excitation wavelength of about 378 nm and a monitoring wavelength of about 543 nm. According to a formula of “I=I₀exp (−t/τ)”, in which I₀ is an initial luminescence intensity, and I is a luminescence intensity related to the afterglow time (τ), a afterglow time of the Ca₃La_(0.95)Tb_(0.05)(PO₄)₃ is about 2.46 ms (the required afterglow time of the luminescent material is about 1 ms-5 ms).

The terbium doped phosphate-based green luminescent material of the exemplary embodiment has a strong absorption of the 172 nm light and has a short fluorescence life time. The Ca₃La_(0.95)Tb_(0.05)(PO₄)₃ has a afterglow time of about 2.46 ms, which is lower than that of the commercial BaAl₁₂O₁₉:Mn. Additionally, the terbium doped phosphate-based green luminescent material in the embodiment has a higher luminescence intensity than that of the commercial BaAl₁₂O₁₉:Mn.

The preparation method of the terbium doped phosphate-based green luminescent material is simply, environmental friendly, easy controlled, and can be commercially processed.

It is believed that the exemplary embodiment and its advantages will be understood from the foregoing description, and it will be apparent that various changes may be made thereto without departing from the spirit and scope of the disclosure or sacrificing all of its advantages, the examples hereinbefore described merely being preferred or exemplary embodiment of the disclosure. 

1. Terbium doped phosphate-based green luminescent material, which has chemical formula of M₃RE_(1-x)Tb_(x)(PO₄)₃, wherein, M is alkaline earth metal, RE is rare-earth element, and x is in a range of 0.001 to
 1. 2. The terbium doped phosphate-based green luminescent material according to claim 1, wherein said rare-earth element RE is at least one of Gd, Y, and La.
 3. The terbium doped phosphate-based green luminescent material according to claim 1, wherein said alkaline earth metal M is at least one of Ca, Sr, and Ba.
 4. The preparation method of terbium doped phosphate-based green luminescent material, comprising: step one, providing the compound used as the source of alkaline earth metal, the compound used as the source of phosphate, the compound used as the source of rare-earth, and the compound used as the source of Tb³⁺ according to the molar ratio of the elements in M₃RE_(1-x)Tb_(x)(PO₄)₃, wherein, the compound used as the source of phosphate is added at excess molar ratio in a range of 10%-30%, M is alkaline earth metal, RE is rare-earth element, and x is in a range of 0.001 to 1; step two, mixing and grinding the compounds to get a mixture; step three, sintering the mixture as pre-treatment, and then cooling the mixture to get a sintered matter; and step four, grinding the sintered matter, calcining the grinded matter in a reducing atmosphere, and then cooling them to get the terbium doped phosphate-based green luminescent material.
 5. Preparation method of terbium doped phosphate-based green luminescent material according to claim 4, wherein the compound used as the source of alkaline earth metal is at least one of alkaline earth oxide, alkaline earth hydroxide, alkaline earth carbonate, and alkaline earth oxalate, the compound used as the source of phosphate is at least one of diammonium phosphate and ammonium dihydrogen phosphate, the compound used as the source of RE³⁺ is rare-earth oxide, rare-earth nitrate, or rare-earth oxalate.
 6. Preparation method of terbium doped phosphate-based green luminescent material according to claim 4, wherein sintering as pre-treatment is carried out at the temperature in a range of 300° C. to 700° C. for 1 hour to 6 hours.
 7. Preparation method of terbium doped phosphate-based green luminescent material according to claim 4, wherein the calcining of step four is twice, the grinded matter is firstly calcined at the temperature in a range of 800° C. to 1500° C. for 4 hours to 24 hours, and then cooled and grinded, after that, a second calcining process is carried out at the temperature in a range of 700° C. to 950° C. for 5 hours to 10 hours, at least one of the first calcining process and the second calcining process is carried out in a reducing atmosphere.
 8. Preparation method of terbium doped phosphate-based green luminescent material according to claim 7, wherein the reducing atmosphere is the mixing gases of nitrogen and hydrogen, the hydrogen, or the carbon monoxide.
 9. Preparation method of terbium doped phosphate-based green luminescent material according to claim 4, wherein said rare-earth element RE is at least one of Gd, Y, and La.
 10. Preparation method of terbium doped phosphate-based green luminescent material according to claim 4, wherein said alkaline earth metal M is at least one of Ca, Sr, and Ba. 